Change of sleep quality from pre- to 3 years post-solid organ transplantation: The Swiss Transplant Cohort Study

Abstract

Background

Poor sleep quality (SQ) is common after solid organ transplantation; however, very little is known about its natural history. We assessed the changes in SQ from pre- to 3 years post-transplant in adult heart, kidney, liver and lung recipients included in the prospective nation-wide Swiss Transplant Cohort Study. We explored associations with selected variables in patients suffering persistent poor SQ compared to those with good or variable SQ.

Methods

Adult single organ transplant recipients enrolled in the Swiss Transplant Cohort Study with pre-transplant and at least 3 post-transplant SQ assessment data were included. SQ was self-reported pre-transplant (at listing), then at 6, 12, 24 and 36 months post-transplant. A single SQ item was used to identify poor (0–5) and good sleepers (6–10). Between organ groups, SQ was compared via logistic regression analysis with generalized estimating equations. Within the group reporting persistently poor SQ, we used logistic regression or Kaplan-Meier analysis as appropriate to check for differences in global quality of life and survival.

Results

In a sample of 1173 transplant patients (age: 52.1±13.2 years; 65% males; 66% kidney, 17% liver, 10% lung, 7% heart) transplanted between 2008 and 2012, pre- transplant poor SQ was highest in liver (50%) and heart (49%) recipients. Overall, poor SQ decreased significantly from pre-transplant (38%) to 24 months post-transplant (26%) and remained stable at 3 years (29%). Patients reporting persistently poor SQ had significantly more depressive symptomatology and lower global quality of life.

Conclusion

Because self-reported poor SQ is related to poorer global quality of life, these results emphasize the need for further studies to find suitable treatment options for poor SQ in transplant recipients.

About the Authors:

Hanna Burkhalter

Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Resources, Validation, Visualization, Writing – original draft

Affiliations Institute of Nursing Science, Department Public Health, University of Basel, Basel, Switzerland, Center of Sleep Medicine, Hirslanden Group, Zürich, Switzerland

ORCID http://orcid.org/0000-0001-7011-0481

Kris Denhaerynck

Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Supervision, Writing – review & editing

Affiliation: Institute of Nursing Science, Department Public Health, University of Basel, Basel, Switzerland

Uyen Huynh-Do

Roles Supervision, Validation, Writing – review & editing

Affiliation: Division of Nephrology and Hypertension, University Hospital of Bern, Bern, Switzerland

Isabelle Binet

Roles Supervision, Validation, Writing – review & editing

Affiliation: Nephrology/Transplantation Medicine, Cantonal Hospital of St.Gallen, St.Gallen, Switzerland

Karine Hadaya

Roles Supervision, Validation, Writing – review & editing

Affiliation: Division of Nephrology and Transplantation, Geneva University Hospital, Geneva, Switzerland

Sabina De Geest

Roles Conceptualization, Funding acquisition, Methodology, Project administration, Resources, Supervision, Validation, Writing – review & editing

* E-mail: [email protected]

Affiliations Institute of Nursing Science, Department Public Health, University of Basel, Basel, Switzerland, Academic Center for Nursing and Midwifery, Department Public Health, KU Leuven, Belgium

for the Psychosocial Interest Group, Swiss Transplant Cohort Study

¶The complete membership of the author group of the Psychosocial Interest Group of the Swiss Transplant Cohort Study can be found in the Acknowledgments.

Abstract

Background

Poor sleep quality (SQ) is common after solid organ transplantation; however, very little is known about its natural history. We assessed the changes in SQ from pre- to 3 years post-transplant in adult heart, kidney, liver and lung recipients included in the prospective nation-wide Swiss Transplant Cohort Study. We explored associations with selected variables in patients suffering persistent poor SQ compared to those with good or variable SQ.

Methods

Adult single organ transplant recipients enrolled in the Swiss Transplant Cohort Study with pre-transplant and at least 3 post-transplant SQ assessment data were included. SQ was self-reported pre-transplant (at listing), then at 6, 12, 24 and 36 months post-transplant. A single SQ item was used to identify poor (0–5) and good sleepers (6–10). Between organ groups, SQ was compared via logistic regression analysis with generalized estimating equations. Within the group reporting persistently poor SQ, we used logistic regression or Kaplan-Meier analysis as appropriate to check for differences in global quality of life and survival.

Results

In a sample of 1173 transplant patients (age: 52.1±13.2 years; 65% males; 66% kidney, 17% liver, 10% lung, 7% heart) transplanted between 2008 and 2012, pre- transplant poor SQ was highest in liver (50%) and heart (49%) recipients. Overall, poor SQ decreased significantly from pre-transplant (38%) to 24 months post-transplant (26%) and remained stable at 3 years (29%). Patients reporting persistently poor SQ had significantly more depressive symptomatology and lower global quality of life.

Conclusion

Because self-reported poor SQ is related to poorer global quality of life, these results emphasize the need for further studies to find suitable treatment options for poor SQ in transplant recipients.

Figures

Table 5

Fig 1

Table 1

Fig 2

Table 2

Table 3

Table 4

Table 5

Fig 1

Table 1

Fig 2

Citation: Burkhalter H, Denhaerynck K, Huynh-Do U, Binet I, Hadaya K, De Geest S, et al. (2017) Change of sleep quality from pre- to 3 years post-solid organ transplantation: The Swiss Transplant Cohort Study. PLoS ONE12(10): e0185036. https://doi.org/10.1371/journal.pone.0185036

Editor: Aric Gregson, University of California Los Angeles, UNITED STATES

Received: December 4, 2016; Accepted: September 4, 2017; Published: October 11, 2017

Copyright: © 2017 Burkhalter et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Data Availability: All relevant data are within the paper.

Funding: The Swiss Transplant Cohort Study is funded by a grant from the Swiss National Research Foundation (Grant number 3347CO-108795). This work is further supported by unrestricted research grants of Astellas (CH & Europe), Roche (CH) and Novartis (CH). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing interests: The Swiss Transplant Cohort Study is funded by a grant from the Swiss National Research Foundation (Grant number 3347CO-108795). This work is further supported by unrestricted research grants from Astellas (CH & Europe), Roche (CH) and Novartis (CH). Their support does not alter our adherence to PLOS ONE policies on sharing data and materials.

Abbreviations: SQ, Sleep Quality; STCS, Swiss Transplant Cohort Study

Background

After a successful transplantation, loss of sleep quality (SQ) typically reduces' recipients' quality of life and may impair survival. However, during follow-up, sleep quality (SQ) self-reports have rarely been collected via standardized protocols. To be feasible, the measurement has to be simple, valid and reliable. Therefore, to differentiate poor from good sleepers, we used a single item from the sleep subscale of the Kidney Disease and Quality of Life–Short Form (KDQoL-SF): “On a scale from 0–10, how would you evaluate your sleep?” Scores of 0–5 were classed as poor; 6–10 indicated good SQ. This item is not yet part of a standardized protocol, and sleep quality is not yet a standardized follow-up criterion.

Poor sleep quality (SQ) is common in hemodialysis patients (49%-53% prevalence) [1, 2]. Kidney transplantation is expected to correct most kidney disease-related abnormalities of the kidney disease and significantly improve the patients’ health. However, a 2011 study reported high (31%) prevalence of poor SQ after kidney transplantation [3]. This may reflect a serious risk regarding patient survival. The Dialysis Outcomes and Practice Patterns Study collected SQ data from 11351 patients in 308 dialysis units across seven countries and reported a 16% higher relative risk of mortality in hemodialysis patients with poor SQ compared to good sleepers [1]. Such a strong link with overall wellbeing and health indicates an equally strong need to detect and understand poor SQ as a post-transplantation health outcome. Patient-reported outcomes (PROs) including SQ are becoming extremely important indicators of the quality of patient care [4]. To date, however, no studies have used PROs (e.g., sleep quality) simultaneously in kidney, heart, liver and lung transplant patients to monitor global quality of life and survival. Data on SQ in kidney, heart, liver and lung transplant patients are scarce, and longitudinal studies are even more so. Therefore, based on data from the Swiss Transplant Cohort Study, the current analysis had three aims: (1) to detect and compare changes in SQ in kidney, heart, liver and lung transplant recipients over time (pre-, 6, 12, 24, and 36 months post-transplant); (2) to compare solid organ transplant recipients groups (kidney, heart, liver and lung) with persistent poor SQ over time; and (3) to compare global quality of life and survival over time (until 3 years post-transplant) in subjects with persistently poor SQ as opposed to those with consistently good and variable SQ.

Materials and methods

Design, sample and setting

For this study we used data from the Swiss Transplant Cohort Study, a prospective open cohort study including 1173 patients transplanted in one of the six Swiss transplant centers (Lausanne, Geneva, Basel, Zürich, Bern, St. Gallen). Details of that study are published elsewhere [5]. Kidney, heart, liver and lung transplant recipients were eligible if they were aged 18 years or older, has received a single transplant (i.e., no multiple-organ transplants) enrolled from May 2, 2008 until February 2, 2012, and were followed up until August 11th, 2015. After providing written informed consent, organ transplant candidates completed the psychosocial questionnaire (socio-demographic, psychosocial, and behavioral variables, including SQ), pre-transplant (at the time of listing), 6 months post-transplant, 1 year post-transplant, and each year thereafter (described elsewhere) [5, 6]. The Swiss Transplant Cohort Study was approved by the ethics committees overseeing the 6 participating transplant centers. None of the transplant recipients received organs from vulnerable populations, as all organ transplantation is regulated by Swiss law. All donors or next of kin freely provided written informed consent.

Variables and measurements

Sleep quality.

Sleep quality (SQ) was assessed with a single item derived from the ‘Kidney Disease Quality of Life–Short Form’ instrument, which was initially developed for patients with end-stage renal disease [1]. Patients were asked, “On a scale of 0 to 10 [where 0 represents ‘very bad’ and 10 represents ‘very good’], how would you rate your sleep quality overall?” Based on ROC curve analysis, values below 6 indicated poor SQ [3]. Therefore, we used <6 as a cut-off to define poor SQ [3]. Content validity was good (content validity index (CVI): .81). Concurrent validity (i.e., in relation to the Pittsburgh Sleep Quality Index (rs: -.737 p < .01)) and discriminant validity (i.e., versus depression diagnosis and the Depression, Anxiety and Stress scale, and quality of life as measured with the EQ-5D) were good [3]. Predictive validity of the SQ item was demonstrated in the Dialysis Outcome and Practice Pattern Study, [1] as poor SQ predicted mortality.

For our second and third aims, we divided patients into two groups based on the longitudinal pattern of their SQ: those who had persistent poor SQ versus all others (transplant recipients with consistently good or variable sleep quality). As at least two post-transplant measurement points were needed to define patients with persistent poor SQ, inclusion was limited to patients who survived at least 1 year post-transplant.

Socio-demographic and clinical variables.

Six socio-demographic variables were extracted from the Swiss Transplant Cohort Study database [5, 6]: gender, age in years at the time of transplantation, transplanted organ (kidney, liver, heart, or lung), time between study inclusion and transplantation, highest completed educational level (never completed high school, high school graduate, some college, college graduate) and marital status (single, married/living together, widow/widower, divorced, separated). We also extracted two clinical variables: main immunosuppressive regimen (Azathioprine, Tacrolimus, Cyclosporine, Rapamune, Mycophenolate Acid) and the two most frequent etiologies of the disease pre-transplant (heart transplant: dilated cardiomyopathy and ischemic heart disease; kidney transplant: glomerulonephritis and polycystic kidney disease; liver transplant: hepatitis C and alcohol; lung transplant: chronic obstructive pulmonary disease and cystic fibrosis).

Depressive symptomatology was assessed via the 7-item depression subscale of the Hospital Anxiety and Depression Scale, a self-reported non-diagnostic screening instrument. This scale is widely used and well-validated as a screening instrument for depression in the general medical population, and, to some extent, in kidney transplantation contexts [7]. The mean scores for depression in a general German population (N = 4410) were 4.8 (males) and 4.7 (females)[8]. Each item is scored on a scale from 0 to 3, with the total score calculated by summing the seven individual item scores (range: 0–21). A cut-off of ≥8 was used to indicate depression [9]. Sensitivity of the HADS depression subscale using this cut-off was 0.86; specificity was 0.81 for depressive disorder screening [10].

Global quality of life was assessed with a visual analogue scale from 0 (worst imaginable quality of life to 100 (best imaginable quality of life). This scale is both widely used and validated for use in German-language settings [6, 11] where it has shown high levels of validity and reliability [12]. The mean score for global quality of life in the general German population was 77.1±17.8 [13]. We used this variable as an outcome as it measures a broad construct of health (a summary of numerous health issues facing transplant recipients) that is close to the transplant recipient’s perspective [12]. Survival was defined as the estimated fraction of transplant recipients who would survive over the six years of the study period, it was used as a function to estimate the probability that transplant recipients with poor SQ would eventually differ from those with consistently good or variable SQ after transplantation.

Statistical analysis

Descriptive analyses of sample characteristics were performed using frequencies, proportions, measures of central tendency (means, medians) and dispersion (standard deviations, interquartile ranges) as appropriate for measurement levels and distributions. Differences in demographic and clinical characteristics among organ groups were screened using Chi-square or Wilcoxon rank-sum tests.

Changes in poor SQ over time for the various organ recipient groups and the overall sample were depicted graphically. They were also modeled via logistic regression analyses using generalized estimating equations to account for the repeated measures [14], and controlling for organ group, age, gender, depressive symptomatology, co-morbidities, immunosuppressive regimen and the time that elapsed between baseline measurement (the pre-transplant psychosocial questionnaire) and transplantation. The model presented was adjusted by retaining only significant covariates.

Two sub-analyses were also performed. The first used an interaction between organ group and time category to generate odds ratio comparisons based entirely on pre-transplant data. The second, performed using post-transplant data, incorporated time as a continuous variable to allow the estimation of linear trends over the post-transplant period. To examine the possible effect of missing follow-up data on model stability, analyses were also performed using a Last-Observation-Carried-Forward (LOCF) imputation strategy.

For our second and third aims, we divided patients into two groups based on their longitudinal sleeping patterns: those who had persistent poor SQ and all others. As at least two post-transplant measurement points were needed to define patients with persistent poor SQ, inclusion was limited to patients who survived at least 1 year post-transplant.

Differences between patients with persistently poor SQ versus those with consistently good or variable SQ were explored via descriptive analyses, and using Chi-square, Wilcoxon rank-sum tests, or Kaplan-Meier estimates as appropriate. We determined both global quality of life and survival via Kaplan Meier analyses, and compared the results with those with consistently good or variable SQ. All analyses were performed using SAS 9.4 (SAS Institute Inc., Cary, NC, USA) software. The alpha level was set at 5%.

Results

Sample characteristics overall

As of February 2, 2012, the Swiss transplant cohort study included 1597 patients, of whom 1173 fulfilled the current study’s inclusion criteria: 770 (65%) kidney, 201 (18%) liver, 123 (10%) lung and 79 (7%) heart transplant candidates. Fig 1 depicts the overall sample size and the number of included respondents per organ group at each data collection point. Demographics and clinical characteristics of the 1173 transplant recipients included in the analyses are provided in Table 1. At pre-transplant measurement, the average patient age was 50.1±13.2 years; almost two-thirds (65.5%) were male; and most (66.1%) were married or living with a partner. The median period between pre-transplant assessment and transplantation was 7.7±9.6 months.

[Figure omitted. See PDF.]

Fig 1. Flow diagram showing the sample as selected from the swiss transplant cohort study overall sample.

https://doi.org/10.1371/journal.pone.0185036.g001

[Figure omitted. See PDF.]

Table 1. Sample characteristics at pre-transplant for all organs and per organ group.

https://doi.org/10.1371/journal.pone.0185036.t001

The follow-up time ranged from 18 months to 7.1 years, with a median of 4.1 years (interquartile range 2.0). Of the 1173 patients included in the study at the pre-transplant measurement, 894 (76.2%) had available data over 36 months. One hundred, eight (9.2%) patients had died by the end of the study.

Of the 765 kidney insufficient patients, 16% (N = 119) were transplanted pre-emptively (estimated GFR (eGFR) was 10 ml/min/1.73m2), 69% (N = 531) were on hemodialysis and 15% (N = 115) on peritoneal dialysis. The mean time on dialysis was 4.0±5.0 years. The eGFR at 36 months was 55 ml/min/1.73m2 post-kidney transplantation and 72 ml/min/1.73m2 post-liver transplantation. The pre-liver-transplantation MELD score was 20±9 and the pre-heart-transplantation Ejection Fraction was 24.4±13.0%.

Changes of poor sleep quality between organ groups over time

Fig 2 shows the percentages of patients with poor SQ at each data collection point. Pre-transplant, 38% of the sample reported poor SQ. At 24 months post-transplant, poor SQ was reported at its lowest level (26%). Fewer heart, kidney and liver transplant recipients reported poor SQ at six months compared to pre-transplant (Table 2). For the kidney and liver transplant groups, this improvement continued until the 1-year measurement. Overall, as illustrated in Table 3, patients’ odds of poor SQ were higher at baseline (OR 1.45; 95%CI: 1.21–1.74) and 6 months post-transplant (OR 1.44; 95%CI: 1.21–1.72) compared to 24 months post-transplant.

[Figure omitted. See PDF.]

Fig 2. Change in poor SQ from pre-transplant to 3 years post-transplant (overall & per transplant group).

https://doi.org/10.1371/journal.pone.0185036.g002

[Figure omitted. See PDF.]

Table 2. Modeling of poor SQ over time and across different organ transplant groups.

https://doi.org/10.1371/journal.pone.0185036.t002

[Figure omitted. See PDF.]

Table 3. Differences in poor SQ over time between organ transplant groups pre-Tx.

https://doi.org/10.1371/journal.pone.0185036.t003

Pre-transplant liver patients reported the highest occurrence of poor SQ (50%), followed closely by heart transplant candidates (49%). Both these groups differed significantly from their lung transplant (32%) and kidney transplant (34%) counterparts (Table 3). A decrease in poor SQ among kidney (OR 0.91; 95%CI: 0.84–0.97; p = 0.005; Table 4) and liver transplant recipients (OR 0.80; 95%CI: 0.69–0.93; p = 0.004) could be observed via linear modeling of post-transplant developments (Table 4). Other organ recipient groups showed no statistically significant changes over time. In terms of estimates and inferences, replacing missing values by imputing the last observed values yearly until the end of the observation period only moderately (not statistically significant) affected the results in any of the tables.

[Figure omitted. See PDF.]

Table 4. Poor SQ over time (in years) with interactions across different organ transplant groups.

https://doi.org/10.1371/journal.pone.0185036.t004

Sample characteristics and correlates for transplant recipients with persistent poor SQ

Table 5 shows the characteristics of the overall sample at 6 months post-transplant, alongside those of persistent poor SQ and of all others (those with consistently good or variable SQ). The persistently poor SQ group accounted for 10% of the sample (N = 107; 10.4%). Poor SQ was more prevalent in patients with lower education (p = 0.03) and in those with more depressive symptoms (p = < .0001).

[Figure omitted. See PDF.]

Table 5. Sample characteristics at pre-transplant overall and per sleep quality pattern.

https://doi.org/10.1371/journal.pone.0185036.t005

Global quality of life and Survival for Patients with persistent poor SQ

Pre-transplant, the global quality of life rating was 55.9±22.6; 6 months post-transplant, it increased to 74.3±17.7. Graft recipients with persistently poor SQ over time had a significantly lower mean global quality of life (59.7±21.5; p = < .0001) compared to those with consistently good or variable SQ. This result was consistent when controlling for organ group, age, gender, comorbidities and time between inclusion in the Swiss Transplant Cohort Study and transplantation. Missing data over time did not change the results (as determined by a sensitivity analysis using a last observation carried forward imputation method). At 6 years post-transplant, survival probability was 0.83 for those with consistently good or variable SQ and 0.79 for patients with persistent poor SQ (not significant).

Discussion

To the best of our knowledge, the current work represents the largest study to date to simultaneously investigate self-reported SQ in heart, lung, liver and kidney transplant groups using a single protocol. We found that poor SQ affected roughly one-third of transplant recipients throughout the measurement period, but generally improved from pre-transplant until 1 year post-transplant. Significant differences in perceived SQ were observed between organ groups. As reported in previous studies, poor SQ is common pre- and post-transplant; however, those studies were limited regarding follow-up periods and sample sizes, and used various SQ assessment methods.

Changes in poor sleep quality over time

The range of poor SQ measured with the Pittsburgh Sleep Quality index is extremely wide in the published studies: 28–69% in heart [15], 8–62% in kidney [3, 15–21] [22], 51–72% in liver [15, 23, 24] and 32–54% in lung transplant recipients [15, 25]. Measured with the Pittsburgh Sleep Quality Index the prevalence of poor SQ in the general population ranges from 22% [26] to 45% [27]. As there are no prevalence data of poor SQ assessed with the single SQ item we cannot conclude that our prevalence is higher than in the general population. The most appropriate conclusion drawn from these results is the comparison of the prevalence of poor SQ across organ transplant groups and over time.

The improvement indicated from pre- to post-kidney transplantation confirms the findings of previous studies [21]. For example, one recent study showed that 46% of kidney transplant recipients experienced a clinically relevant improvement in overall sleep quality, while 21% experienced a clinically relevant deterioration [21] over 5 years of follow up. Over time, kidney and liver transplant recipients showed a significant decrease in poor SQ. The drop might be connected with the normalization of life with a transplanted organ and return to work [28]. Compared to heart and lung groups [29], the fear of rejection and the frequency of follow-up visits are normally reduced at 36 months post-kidney and liver transplantation. Liaveri et.al.’s study in renal transplant recipients reported improved quality of life after transplantation; however this benefit does not seem to extend to sleep quality [30]. In that case, sleep quality was affected by frequency of post-traumatic stress symptoms, depression, restless leg syndrome, high diastolic blood pressure, and pain [30].

One hypothesis to explain these connections is that fatigue (reported prevalence post-kidney transplantation: 40%-50% [31]) interferes with perceived sleep quality. It also limits a person's ability to carry out ordinary daily activities, with a bidirectional impact on sleep [32]. Daytime sleepiness improves [22] after kidney transplantation; however, those for whom it persists are more prone to immunosuppression non-adherence [33]. No [22] or little improvement [34] was found with objective measurements such as melatonin secretion or circadian rhythms.

No significant change over time was found in heart and lung transplant recipients. Their slope showed fluctuation that could represent the health instability in these transplant recipients. In a qualitative study the recipients’ uncertainty reflected their complex medication regimens, unpredictable future health/prognosis, and complex role and identity challenges [35]. Heart and lung transplant recipients’ medication regimen may also be more complex than those of liver and kidney recipients [36, 37].

Characteristics of transplant recipients with persistent poor SQ over time

Transplant recipients with persistent poor SQ (10% of the sample) need to consult with a sleep medicine expert. Occasionally, not getting enough sleep is completely normal; however, over months and years, poor SQ results in a suffering trajectory. E.g., we found that transplant recipients with persistent poor SQ score significantly higher on the depressive symptomatology scale. This association mainly corroborates previous findings [38, 39] in transplant recipients. Among patients with lower educational levels and more depressive symptomatology, the predisposition for poor SQ has previously been confirmed by Patel et. al. [40] and in a review by Tsuno et.al. [41].

Transplant recipients whose poor SQ persisted over extended periods had a significantly lower mean global quality of life compared to those with consistently good or variable sleep quality. A study including patients suffering from chronic illnesses such as coronary artery disease showed that both sleep quality and sleep quantity impact these patients´ quality of life [42]. This is congruent with a recent review´s finding that pronounced persistent poor sleep is a major risk for psychiatric, cardiovascular, metabolic or hormonal co-morbidity and mortality [43].

We found no increased mortality risk among transplant recipients whose poor SQ persisted over time. Poor SQ, depression and poor global quality of life commonly co-occur in transplant recipients in ways that suggest bi-directional influence. Evidence that poor SQ is part of a cluster of symptoms has been found in cancer patients [44]. However, further studies are needed as a recent study (N = 152 renal transplant recipients) reported an amelioration of renal function post-transplantation that improved several aspects of quality of life, but with no beneficial effect on self-reported sleep [30]. Finally, as the high prevalence of poor SQ is an increasing public health issue [45], its associations with poorer outcomes indicate a need for regular assessment.

Clinical relevance and possible interventions

Of the sleep assessment methods currently available, self-reporting is the most accessible, least expensive and simplest to integrate into daily clinical practice [1, 3]. Our analysis showed no association between poor SQ and lower survival; however, the dialysis Outcome and Practice Patterns Study associated poor SQ with higher mortality [1]. Therefore, it is worth integrating this simple question into standard follow-up care while monitoring other parameters.

If during the follow-up visit a score >6 on the single-item self-report of SQ is given, a more in-depth questionnaire or a sleep assessment-asking among other things, about sleep aids should follow. Transplant recipients are educated not to take over-the-counter medicines or herbal supplements without first discussing them with the transplant clinician [46]. In the general population, use of over-the-counter sleep aids (e.g., herbal pills, melatonin or antihystamines) is common [47]. However herbal formulations with an anxiolytic and sedative effect might precipitate liver failure [48]. Even in healthy people, sleep aids are always potentially toxic to the kidneys and liver [49], with common adverse effects including daytime somnolence or decreased alertness [50]. Additional risks have to be acknowledged for all transplant patients. To deal with the problem of persistent poor sleep quality, though, it is crucial to know which factors or combinations of factors influence patients’ perceptions of their SQ. To understand these factors and move forward, system-level improvement is needed in transplant recipient follow-up care.

Strength and limitation

A limitation of the Swiss Transplant Cohort Study, is that, in the interests of their instrument´s overall feasibility, its designers could include only a very short and quick scale on SQ. Compared to a well-established tool such as the Pittsburgh Sleep Quality Index, our single-item solution is a weak measurement of sleep quality. As a counterpoint, the Swiss Transplant Cohort Study includes a large sample of solid organ transplant recipients reporting sleep quality issues over time.

One further weakness is that the Swiss Transplant Cohort Study psychosocial questionnaire does not permit investigation of specific sleep disorders such as restless leg syndrome, periodic limb movement, or sleep apnea. However this single-item scale´s validity has been confirmed in kidney studies, suggesting further uses in the clinical context of organ transplantation [1–3]. This single-item SQ measurement could easily be incorporated in ambulatory clinic follow-up care for transplant recipients.

Conclusion

Sleep quality improved following transplantation; but poor sleep quality was prevalent in kidney, heart, liver and lung transplanted patients. Therefore, SQ should be assessed routinely in solid organ transplant recipients.

Acknowledgments

The results presented in this paper have not been published previously in whole or part, except in abstract form: Burkhalter H., Denhaerynck K., De Geest S., (June 2nd-6th 2012). Sleep quality improves from time of listing to 2 years post- transplant in solid organ transplant recipients: a prospective cohort study, poster presentation (Poster session Disparities to Outcome and Access 729) at the American Transplant Congress, Boston, MA.

We extend our full appreciation to the swiss transplant cohort study core team, the Psychosocial Interest Group of the swiss transplant cohort study and to the 6 Swiss transplant centers for supporting our research. We also thank Chris Shultis for editing and proof reading the manuscript. The authors have no conflicts of interest regarding the data presented in this manuscript. This study has been conducted in the framework of the Swiss Transplant Cohort Study, supported by the Swiss National Science Foundation and the Swiss University Hospitals (G15) and transplant centers.

^The members of the Psychosocial Interest Group are: Lut Berben, Hanna Burkhalter, Veerle Claes, Sabina De Geest, Kris Denhaerynck, Remon Helmy, Monika Kirsch, Lynn Leppla, Oliver Mauthner, Marian Struker (University of Basel); Annette Boehler, Sabine Gerull, Michael T Koller (University Hospital Basel); Uyen Huynh-Do (University Hospital Inselspital Bern); Elsa Boely (University Hospital Geneva); Emmanuelle Catana (University Hospital Lausanne); Amira Simcox (University of Lausanne); Annina Seiler, Richard Klaghofer (University Hospital Zurich); Isabelle Binet, Patrizia Künzler-Heule (Cantonal Hospital St. Gallen); Sonja Beckmann (University of Basel, University Hospital Zurich)

^ The members of the Swiss Transplant Cohort Study are: Rita Achermann, Patrizia Amico, John-David Aubert, Vanessa Banz, Guido Beldi, Christian Benden, Christoph Berger, Isabelle Binet, Pierre-Yves Bochud, Heiner Bucher, Thierry Carell, Emmanuelle Catana, Yves Chalandon, Sabina de Geest, Olivier de Rougemont, Michael Dickenmann, Michel Duchosal, Laure Elkrief, Thomas Fehr, Sylvie Ferrari-Lacraz, Christian Garzoni, Paola Gasche Soccal, Christophe Gaudet, Emiliano Giostra, Déla Golshayan, Karine Hadaya, Jörg Halter, Dominik Heim, Christoph Hess, Sven Hillinger, Hans H. Hirsch, Günther Hofbauer, Uyen Huynh-Do, Franz Immer, Richard Klaghofer, Michael Koller (Head of the data center), Bettina Laesser, Roger Lehmann, Christian Lovis, Pietro Majno; Oriol Manuel, Hans-Peter Marti, Pierre Yves Martin, Pascal Meylan, (Head, Biological samples management group), Paul Mohacsi, Philippe Morel, Ulrike Mueller, Nicolas J Mueller (Chairman Scientific Committee), Helen Mueller-McKenna (Head of local data management), Antonia Müller, Thomas Müller, Beat Müllhaupt, David Nadal, Manuel Pascual (Executive office), Jakob Passweg, Juliane Rick, Eddy Roosnek, Anne Rosselet, Silvia Rothlin, Frank Ruschitzka, Urs Schanz, Stefan Schaub, Aurelia Schnyder, Christian Seiler, Susanne Stampf, Jürg Steiger (Head, Executive Office), Guido Stirnimann, Christian Toso, Christian Van Delden (Executive office), Jean-Pierre Venetz, Jean Villard, Madeleine Wick (STCS coordinator), Markus Wilhelm, Patrick Yerly.

Citation: Burkhalter H, Denhaerynck K, Huynh-Do U, Binet I, Hadaya K, De Geest S, et al. (2017) Change of sleep quality from pre- to 3 years post-solid organ transplantation: The Swiss Transplant Cohort Study. PLoS ONE12(10): e0185036. https://doi.org/10.1371/journal.pone.0185036

References

1. Elder SJ, Pisoni RL, Akizawa T, Fissell R, Andreucci VE, Fukuhara S, et al. Sleep quality predicts quality of life and mortality risk in haemodialysis patients: results from the Dialysis Outcomes and Practice Patterns Study (DOPPS). Nephrol Dial Transplant. 2008;23(3):998–1004. pmid:17911092.

2. Brekke FB, Waldum B, Amro A, Osthus TB, Dammen T, Gudmundsdottir H, et al. Self-perceived quality of sleep and mortality in Norwegian dialysis patients. Hemodial Int. 2014;18(1):87–94. pmid:23841517.

3. Burkhalter H, Sereika SM, Engberg S, Wirz-Justice A, Steiger J, De Geest S. Validity of 2 sleep quality items to be used in a large cohort study of kidney transplant recipients. Prog Transpl. 2011;21(1):27–35. Epub 2011/04/14. pmid:21485940.

4. Snyder CF, Aaronson NK, Choucair AK, Elliott TE, Greenhalgh J, Halyard MY, et al. Implementing patient-reported outcomes assessment in clinical practice: a review of the options and considerations. Qual Life Res. 2012;21(8):1305–14. pmid:22048932.

5. Koller MT, van Delden C, Muller NJ, Baumann P, Lovis C, Marti HP, et al. Design and methodology of the Swiss Transplant Cohort Study (STCS): a comprehensive prospective nationwide long-term follow-up cohort. Eur J Epidemiol. 2013;28(4):347–55. pmid:23546766; PubMed Central PMCID: PMC3653038.

6. De Geest S, Burkhalter H, Berben L, Bogert LJ, Denhaerynck K, Glass TR, et al. The Swiss Transplant Cohort Study's framework for assessing lifelong psychosocial factors in solid-organ transplants. Prog Transplant. 2013;23(3):235–46. pmid:23996943.

7. Bjelland I, Dahl AA, Haug TT, Neckelmann D. The validity of the Hospital Anxiety and Depression Scale. An updated literature review. J Psych Res. 2002;52(2):69–77. pmid:11832252.

8. Hinz A, Brahler E. Normative values for the hospital anxiety and depression scale (HADS) in the general German population. J Psychosom Res. 2011;71(2):74–8. pmid:21767686.

9. Noohi S, Karami GR, Lorgard-Dezfuli-Nejad M, Najafi M, Saadat SH. Are all domains of quality of life poor among elderly kidney recipients? Transplant Proc. 2007;39(4):1079–81. pmid:17524896.

10. Vodermaier A, Millman RD. Accuracy of the Hospital Anxiety and Depression Scale as a screening tool in cancer patients: a systematic review and meta-analysis. Support Care Cancer. 2011;19(12):1899–908. pmid:21898134.

11. Kugler C, Gottlieb J, Warnecke G, Schwarz A, Weissenborn K, Barg-Hock H, et al. Health-related quality of life after solid organ transplantation: a prospective, multiorgan cohort study. Transplantation. 2013;96(3):316–23. pmid:23715048.

12. Feng Y, Parkin D, Devlin NJ. Assessing the performance of the EQ-VAS in the NHS PROMs programme. Qual Life Res. 2014;23(3):977–89. pmid:24081873; PubMed Central PMCID: PMCPMC4287662.

13. Hinz A, Klaiberg A, Brahler E, Konig HH. [The Quality of Life Questionnaire EQ-5D: modelling and norm values for the general population]. Psychotherapie, Psychosomatik und Medizinische Psychologie. 2006;56(2):42–8. pmid:16453241.

14. Liang KY, Zeger SL. Longitudinal Data Analysis Using Generalized Linear Models. Biometrika. 1986;73(1):13–22.

15. Reilly-Spong M, Park T, Gross CR. Poor sleep in organ transplant recipients: self-reports and actigraphy. Clin Transplant. 2013;27(6):901–13. pmid:24118416; PubMed Central PMCID: PMC3855625.

16. Silva DS, Andrade Edos S, Elias RM, David-Neto E, Nahas WC, Castro MC. The perception of sleep quality in kidney transplant patients during the first year of transplantation. Clinics. 2012;67(12):1365–71. Epub 2013/01/09. pmid:23295588; PubMed Central PMCID: PMC3521797.

17. Kachuee H, Ameli J, Taheri S, Assari S, Riahipour F, Khedmat H, et al. Sleep quality and its correlates in renal transplant patients. Transplant Proc. 2007;39(4):1095–7. pmid:17524901.

18. Liu HX, Lin J, Lin XH, Wallace L, Teng S, Zhang SP, et al. Quality of sleep and health-related quality of life in renal transplant recipients. International journal of clinical and experimental medicine. 2015;8(9):16191–8. pmid:26629133; PubMed Central PMCID: PMC4659022.

19. Burkhalter H, Wirz-Justice A, Cajochen C, Weaver T, Steiger J, Fehr T, et al. Validation of a single item to assess daytime sleepiness for the Swiss Transplant Cohort Study. Prog Transplant. 2013;23(3):220–8. pmid:23996941.

20. Eryilmaz MM, Ozdemir C, Yurtman F, Cilli A, Karaman T. Quality of sleep and quality of life in renal transplantation patients. Transplant Proc. 2005;37(5):2072–6. pmid:15964342.

21. Brekke FB, Waldum-Grevbo B, von der Lippe N, Os I. The effect of renal transplantation on quality of sleep in former dialysis patients. Transpl Int. 2017;30(1):49–56. pmid:27696543.

22. Russcher M, Nagtegaal JE, Nurmohamed SA, Koch BC, van der Westerlaken MM, van Someren EJ, et al. The effects of kidney transplantation on sleep, melatonin, circadian rhythm and quality of life in kidney transplant recipients and living donors. Nephron. 2015;129(1):6–15. pmid:25531829.

23. Rodrigue JR, Nelson DR, Reed AI, Hanto DW, Curry M. Fatigue and sleep quality before and after liver transplantation. Prog Transplant. 2010;20(3):221–33. Epub 2010/10/12. pmid:20929106.

24. van Ginneken BT, van den Berg-Emons RJ, van der Windt A, Tilanus HW, Metselaar HJ, Stam HJ, et al. Persistent fatigue in liver transplant recipients: a two-year follow-up study. Clin Transplant. 2010;24(1):E10–6. Epub 2009/09/12. CTR1083 [pii] pmid:19744096.

25. Fatigati A, Alrawashdeh M, Zaldonis J, Dabbs AD. Patterns and Predictors of Sleep Quality Within the First Year After Lung Transplantation. Prog Transplant. 2016;26(1):62–9. pmid:27136251.

26. Furihata R, Uchiyama M, Takahashi S, Suzuki M, Konno C, Osaki K, et al. The association between sleep problems and perceived health status: a Japanese nationwide general population survey. Sleep medicine. 2012;13(7):831–7. pmid:22609021.

27. Lacruz ME, Schmidt-Pokrzywniak A, Dragano N, Moebus S, Deutrich SE, Mohlenkamp S, et al. Depressive symptoms, life satisfaction and prevalence of sleep disturbances in the general population of Germany: results from the Heinz Nixdorf Recall study. BMJ open. 2016;6(1):e007919. pmid:26729376.

28. Eppenberger L, Hirt-Minkowski P, Dickenmann M. Back to work? Socioeconomic status after kidney transplantation. Swiss medical weekly. 2015;145:w14169. pmid:26219088.

29. Xu J, Adeboyejo O, Wagley E, Aubrecht J, Song MK, Thiry L, et al. Daily burdens of recipients and family caregivers after lung transplant. Prog Transplant. 2012;22(1):41–7; quiz 8. pmid:22489442; PubMed Central PMCID: PMCPMC3331720.

30. Liaveri PG, Dikeos D, Ilias I, Lygkoni EP, Boletis IN, Skalioti C, et al. Quality of sleep in renal transplant recipients and patients on hemodialysis. J Psychosom Res. 2017;93:96–101. pmid:28107900.

31. Bossola M, Pepe G, Vulpio C. Fatigue in kidney transplant recipients. Clin Transplant. 2016;30(11):1387–93. pmid:27622392.

32. Monk TH. Practical consequences of fatigue-related performance failures. Sleep. 2007;30(11):1402–3. pmid:18041474; PubMed Central PMCID: PMCPMC2082096.

33. Burkhalter H, Wirz-Justice A, Cajochen C, Weaver TE, Steiger J, Fehr T, et al. Daytime sleepiness in renal transplant recipients is associated with immunosuppressive non-adherence: a cross-sectional, multi-center study. Clin Transplant. 2014;28(1):58–66. pmid:24325281.

34. Burkhalter H, Geest S, Wirz-Justice A, Cajochen C. Melatonin rhythms in renal transplant recipients with sleep-wake disturbances. Chronobiol Int. 2016:1–11. pmid:27101434.

35. Martin SC, Stone AM, Scott AM, Brashers DE. Medical, personal, and social forms of uncertainty across the transplantation trajectory. Qual Health Res. 2010;20(2):182–96. pmid:19955227.

36. Bryant BM, Libby AM, Metz KR, Page RL 2nd, Ambardekar AV, Lindenfeld J, et al. Evaluating Patient-Level Medication Regimen Complexity Over Time in Heart Transplant Recipients. Ann Pharmacother. 2016;50(11):926–34. pmid:27371949.

37. Kamila P, Smith SG, Patzer R, Wolf MS, Marina S. Medication regimen complexity in kidney and liver transplant recipients. Transplantation. 2014;98(7):e73–4. pmid:25285955; PubMed Central PMCID: PMCPMC4187107.

38. Noohi S, Khaghani-Zadeh M, Javadipour M, Assari S, Najafi M, Ebrahiminia M, et al. Anxiety and depression are correlated with higher morbidity after kidney transplantation. Transplant Proc. 2007;39(4):1074–8. pmid:17524895.

39. Sabbatini M, Pisani A, Crispo A, Nappi R, Gallo R, Cianciaruso B, et al. Renal transplantation and sleep: a new life is not enough. J Nephrol. 2008;21 Suppl 13:S97–101. pmid:18446740.

40. Patel NP, Grandner MA, Xie D, Branas CC, Gooneratne N. "Sleep disparity" in the population: poor sleep quality is strongly associated with poverty and ethnicity. BMC Public Health. 2010;10:475. pmid:20701789; PubMed Central PMCID: PMCPMC2927542.

41. Tsuno N, Besset A, Ritchie K. Sleep and depression. J Clin Psychiatry. 2005;66(10):1254–69. pmid:16259539.

42. Edell-Gustafsson UM, Gustavsson G., Yngman Uhlin P. Effects of sleep loss in men and women with insufficient sleep suffering from chronic disease: a model for supportive nursing care. Int J Nurs Pract. 2003;9(1):49–59. pmid:12588620.

43. Garbarino S, Lanteri P, Durando P, Magnavita N, Sannita WG. Co-Morbidity, Mortality, Quality of Life and the Healthcare/Welfare/Social Costs of Disordered Sleep: A Rapid Review. Int J Environ Res Public Health. 2016;13(8). pmid:27548196; PubMed Central PMCID: PMC4997517.

44. Fiorentino L, Rissling M, Liu L, Ancoli-Israel S. The Symptom Cluster of Sleep, Fatigue and Depressive Symptoms in Breast Cancer Patients: Severity of the Problem and Treatment Options. Drug Discov Today Dis Models. 2011;8(4):167–73. pmid:22140397; PubMed Central PMCID: PMCPMC3228259.

45. Institute of Medicine (US) Committee on Sleep Medicine and Research. Functional and Economic Impact of Sleep Loss and Sleep-Related Disorders,. In: Colten HR, Altevogt BM, editors. Sleep Disorders and Sleep Deprivation: An Unmet Public Health Problem. The National Academies Collection: Reports funded by National Institutes of Health. Washington (DC)2006.

46. International Transplant Nusse Society. Transplant Patient Educational Booklets: International Transplant Nusse Society,; 2017 [cited 2017 4th, January]. Available from: http://www.itns.org/patienteducation.html.

47. Abraham O, Schleiden LJ, Brothers AL, Albert SM. Managing sleep problems using non-prescription medications and the role of community pharmacists: older adults' perspectives. Int J Pharm Pract. 2017. pmid:28261882.

48. Shi Y, Dong JW, Zhao JH, Tang LN, Zhang JJ. Herbal Insomnia Medications that Target GABAergic Systems: A Review of the Psychopharmacological Evidence. Curr Neuropharmacol. 2014;12(3):289–302. pmid:24851093; PubMed Central PMCID: PMCPMC4023459.

49. Gabardi S, Luu L. Nonprescription analgesics and their use in solid-organ transplantation: a review. Prog Transplant. 2004;14(3):182–90. pmid:15495777.

50. Schroeck JL, Ford J, Conway EL, Kurtzhalts KE, Gee ME, Vollmer KA, et al. Review of Safety and Efficacy of Sleep Medicines in Older Adults. Clin Ther. 2016;38(11):2340–72. pmid:27751669.